Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24